SG2014011654A - Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof - Google Patents
Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereofInfo
- Publication number
- SG2014011654A SG2014011654A SG2014011654A SG2014011654A SG2014011654A SG 2014011654 A SG2014011654 A SG 2014011654A SG 2014011654 A SG2014011654 A SG 2014011654A SG 2014011654 A SG2014011654 A SG 2014011654A SG 2014011654 A SG2014011654 A SG 2014011654A
- Authority
- SG
- Singapore
- Prior art keywords
- kynurenine
- methods
- pharmaceutical compositions
- monooxygenase inhibitors
- monooxygenase
- Prior art date
Links
- 102100037652 Kynurenine 3-monooxygenase Human genes 0.000 title 1
- 108010033242 Kynurenine 3-monooxygenase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicinal Preparation (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161529003P | 2011-08-30 | 2011-08-30 | |
| PCT/US2012/052617 WO2013033068A1 (fr) | 2011-08-30 | 2012-08-28 | Inhibiteurs de kynurénine-3-monooxygénase, compositions pharmaceutiques et procédés d'utilisation de ces compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG2014011654A true SG2014011654A (en) | 2014-08-28 |
Family
ID=47756801
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2014011654A SG2014011654A (en) | 2011-08-30 | 2012-08-28 | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US9428464B2 (fr) |
| EP (1) | EP2751086A4 (fr) |
| JP (1) | JP2014525443A (fr) |
| KR (1) | KR20140072037A (fr) |
| CN (1) | CN103827095A (fr) |
| AR (1) | AR087711A1 (fr) |
| AU (1) | AU2012300246A1 (fr) |
| BR (1) | BR112014004845A2 (fr) |
| CA (1) | CA2844521A1 (fr) |
| EA (1) | EA201490279A1 (fr) |
| HK (1) | HK1199726A1 (fr) |
| IL (1) | IL231271A0 (fr) |
| MX (1) | MX2014002459A (fr) |
| PH (1) | PH12014500472A1 (fr) |
| SG (1) | SG2014011654A (fr) |
| TW (1) | TW201326138A (fr) |
| WO (1) | WO2013033068A1 (fr) |
| ZA (1) | ZA201401117B (fr) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2732806A1 (fr) * | 2008-08-04 | 2010-02-11 | John Wityak | Certains inhibiteurs de kynurenine-3-monooxygenase, compositions pharmaceutiques, et procedes d'utilisation de ceux-ci |
| WO2013016488A1 (fr) * | 2011-07-28 | 2013-01-31 | Celia Dominguez | Certains inhibiteurs de kynurénine-3-mono-oxygénase, compositions pharmaceutiques et leurs procédés d'utilisation |
| WO2013033068A1 (fr) | 2011-08-30 | 2013-03-07 | Stephen Martin Courtney | Inhibiteurs de kynurénine-3-monooxygénase, compositions pharmaceutiques et procédés d'utilisation de ces compositions |
| SI2750677T1 (sl) * | 2011-08-30 | 2017-10-30 | Chdi Foundation, Inc. | Inhibitorji kinurenin-3-monooksigenaze, farmacevtski sestavki in postopki njihove uporabe |
| MY191366A (en) * | 2013-03-13 | 2022-06-20 | Forma Therapeutics Inc | Novel compounds and compositions for inhibition of fasn |
| US10258621B2 (en) * | 2014-07-17 | 2019-04-16 | Chdi Foundation, Inc. | Methods and compositions for treating HIV-related disorders |
| AU2015328174B2 (en) | 2014-10-06 | 2020-05-21 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
| UA120381C2 (uk) * | 2014-12-19 | 2019-11-25 | Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед | 3-(6-АЛКОКСИ-5-ХЛОРБЕНЗО[d]ІЗОКСАЗОЛ-3-ІЛ)ПРОПАНОВА КИСЛОТА, ЗАСТОСОВНА ЯК ІНГІБІТОРИ КІНУРЕНІНМОНООКСИГЕНАЗИ |
| GB201508864D0 (en) * | 2015-05-22 | 2015-07-01 | Glaxosmithkline Ip Dev Ltd | Compounds |
| RS62639B1 (sr) | 2015-07-06 | 2021-12-31 | Alkermes Inc | Hetero-halo inhibitori histonskih deacetilaza |
| US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
| AU2017240685B2 (en) | 2016-03-31 | 2021-08-12 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
| JOP20190042B1 (ar) | 2016-09-30 | 2021-08-17 | Vertex Pharma | مُعدِّل لمنظم موصلية التليف الكيسي عبر الغشاء، وتركيبات صيدلانية، وطرق للعلاج، وعملية لتصنيع المُعدِّل |
| MA46649A (fr) | 2016-10-13 | 2019-08-21 | Juno Therapeutics Inc | Méthodes et compositions d'immunothérapie impliquant des modulateurs de la voie métabolique du tryptophane |
| JOP20190125B1 (ar) | 2016-12-09 | 2022-03-14 | Vertex Pharma | مُعدِّل لمنظم موصلية التليف الكيسي عبر الغشاء، وتركيبات صيدلانية، وطرق للعلاج، وعملية لتصنيع المُعدِّل |
| MD3570834T2 (ro) | 2017-01-11 | 2022-04-30 | Alkermes Inc | Inhibitori biciclici ai histon deacetilazei |
| EP3634402A1 (fr) | 2017-06-08 | 2020-04-15 | Vertex Pharmaceuticals Incorporated | Méthodes de traitement de la fibrose kystique |
| AU2018304168B2 (en) | 2017-07-17 | 2023-05-04 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
| US11434201B2 (en) | 2017-08-02 | 2022-09-06 | Vertex Pharmaceuticals Incorporated | Processes for preparing pyrrolidine compounds |
| JP7152471B2 (ja) | 2017-08-07 | 2022-10-12 | ロダン・セラピューティクス,インコーポレーテッド | ヒストン脱アセチル化酵素の二環阻害剤 |
| US10654829B2 (en) | 2017-10-19 | 2020-05-19 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of CFTR modulators |
| CA3085006A1 (fr) | 2017-12-08 | 2019-06-13 | Vertex Pharmaceuticals Incorporated | Procedes pour preparer des modulateurs du regulateur de la conductance transmembranaire de la mucoviscidose |
| TWI810243B (zh) | 2018-02-05 | 2023-08-01 | 美商維泰克斯製藥公司 | 用於治療囊腫纖化症之醫藥組合物 |
| EP3774825A1 (fr) | 2018-04-13 | 2021-02-17 | Vertex Pharmaceuticals Incorporated | Modulateurs du régulateur de la conductance transmembranaire de la fibrose kystique, compositions pharmaceutiques, procédés de traitement et procédé de fabrication du modulateur |
| EP3852879A1 (fr) | 2018-09-21 | 2021-07-28 | Pfizer Inc. | Dioxocyclobuténylamino-3-hydroxy-picolinamides n-substitués utiles en tant qu'inhibiteurs de ccr6 |
| TWI767148B (zh) | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | 抑制脂肪酸合成酶(fasn) |
| US10793554B2 (en) | 2018-10-29 | 2020-10-06 | Forma Therapeutics, Inc. | Solid forms of 4-(2-fluoro-4-(1-methyl-1H-benzo[d]imidazol-5-yl)benzoyl)piperazin-1-yl)(1-hydroxycyclopropyl)methanone |
| CN110128346A (zh) * | 2019-05-17 | 2019-08-16 | 南开大学 | 一类联芳酰胺吡唑衍生物及其制备方法和用途 |
| EP4171221A4 (fr) * | 2020-06-29 | 2024-07-24 | University of Notre Dame du Lac | Composés de picolinamide antibactériens |
| JP2023536886A (ja) * | 2020-08-06 | 2023-08-30 | シーエイチディーアイ ファウンデーション,インコーポレーテッド | ハンチンチンタンパク質をイメージングするためのヘテロビアリール化合物及びイメージング剤 |
| US20230391752A1 (en) * | 2020-10-22 | 2023-12-07 | Chulalongkorn University | Pyrrolidine-3-carboxamide derivatives and related uses |
| US12029718B2 (en) | 2021-11-09 | 2024-07-09 | Cct Sciences, Llc | Process for production of essentially pure delta-9-tetrahydrocannabinol |
| WO2023114977A1 (fr) * | 2021-12-16 | 2023-06-22 | Tiaki Therapeutics, Inc. | Antagonistes du récepteur s1pr4 et leurs procédés d'utilisation |
Family Cites Families (123)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3908012A (en) | 1970-10-05 | 1975-09-23 | Pfizer | Arylpyrimidines-inhibitors of platelet aggregation and bronchodilators |
| US3707560A (en) | 1970-10-05 | 1972-12-26 | Pfizer | Certain 4-amino-6-aryl-pyrimidines |
| FR2204406A1 (en) | 1972-10-26 | 1974-05-24 | Delalande Sa | 1-Phenyl-3-aminocarbonylpropan-1-one oxime carbamates - with analgesic, antiinflammatory, hypotensive and sedative activities etc. |
| US3950525A (en) | 1973-06-19 | 1976-04-13 | Pfizer Inc. | Relaxation of smooth muscle in a mammal |
| US3935202A (en) | 1974-03-18 | 1976-01-27 | American Home Products Corporation | 3-(4-biphenylylcarbonyl)propionamido cephalosporin derivatives |
| US4634689A (en) | 1985-10-31 | 1987-01-06 | Schering Corporation | Phosphinylalkanoyl imino acids |
| DE3609596A1 (de) | 1986-03-21 | 1987-10-01 | Hoechst Ag | 2-azolylmethyl-2-aryl-1,3-dioxolane und deren salze, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung |
| JPH0788357B2 (ja) | 1986-10-27 | 1995-09-27 | 吉富製薬株式会社 | ピペラジン化合物 |
| JPH01113377A (ja) | 1987-10-23 | 1989-05-02 | Yoshitomi Pharmaceut Ind Ltd | ピペラジン化合物 |
| MX16687A (es) | 1988-07-07 | 1994-01-31 | Ciba Geigy Ag | Compuestos de biarilo y procedimiento para su preparacion. |
| US5102904A (en) | 1989-12-08 | 1992-04-07 | American Cyanamid Company | N-oxygenated arylpyrrole insecticidal, acaricidal and nematicidal agents and use thereas |
| AU644159B2 (en) | 1990-05-17 | 1993-12-02 | Novartis Ag | 2-anilino-4-cyanopyrimidine derivatives |
| DE4103695A1 (de) | 1991-02-07 | 1992-08-13 | Basf Ag | Oximether und diese enthaltende fungizide |
| US5334720A (en) | 1991-03-07 | 1994-08-02 | Fisons Corporation | Diphenyl-1-(aminoalkyl)-2-piperidinone and -2-pyrrolidinone derivatives having anticonvulsant properties |
| WO1995023135A1 (fr) | 1991-03-07 | 1995-08-31 | Fisons Corporation | Derives de diphenyl-2-piperidinone et -2-pyrrolidinone possedant une activite anticonvulsivante et neuroprotectrice |
| JPH0741459A (ja) | 1993-07-29 | 1995-02-10 | Sumitomo Pharmaceut Co Ltd | 新規エラスターゼ阻害剤 |
| DE59409322D1 (de) | 1993-12-03 | 2000-06-08 | Hoffmann La Roche | Essigsäurederivate als Arzneimittel |
| US5338739A (en) | 1994-03-10 | 1994-08-16 | Hoechst-Roussel Pharmaceuticals Inc. | (Pyrrolidinyl)phenyl carbamates, compositions and use |
| DE4430639A1 (de) * | 1994-08-29 | 1996-03-07 | Bayer Ag | Verwendung von 5-substituierten Pyridin- und Hexahydrochinolin-3-carbonsäurederivaten |
| FR2732017B1 (fr) | 1995-03-21 | 2000-09-22 | Inst Nat Sante Rech Med | Nouveaux derives de l'imidazole antagonistes et/ou agonistes du recepteur h3 de l'histamine, leur preparation et leurs applications therapeutiques |
| BR9611723A (pt) | 1995-11-17 | 1999-06-01 | Bayer Ag | Bifenil éter-oxazolinas |
| JP2000502343A (ja) | 1995-12-22 | 2000-02-29 | ワーナー―ランバート・コンパニー | マトリックスメタロプロテイナーゼのインヒビターとしての芳香族ケト酸およびその誘導体 |
| DE19600934A1 (de) | 1996-01-12 | 1997-07-17 | Basf Ag | Substituierte Aza- und Diazacycloheptan- und Cyclooctanverbindungen und deren Verwendung |
| EP0927156A1 (fr) | 1996-09-04 | 1999-07-07 | Warner-Lambert Company | Acides biphenyl-butyriques et leurs derives, utilises comme inhibiteurs des metalloproteases de matrice |
| CA2263886A1 (fr) | 1996-12-09 | 1998-06-18 | Warner-Lambert Company | Procede destine a traiter et a prevenir l'insuffisance cardiaque et la dilatation ventriculaire |
| DK0946166T3 (da) | 1996-12-17 | 2004-05-03 | Warner Lambert Co | Anvendelse af matrixmetalloproteinaseinhibitorer til fremme af sårheling |
| JP2001511813A (ja) * | 1997-02-18 | 2001-08-14 | ニューロクライン バイオサイエンシーズ,インコーポレイテッド | Crfレセプターアンタゴニストおよびそれらに関連する方法 |
| US5925639A (en) | 1997-06-17 | 1999-07-20 | Schering Corporation | Keto amide derivatives useful as farnesyl protein transferase inhibitors |
| WO1999018079A1 (fr) | 1997-10-06 | 1999-04-15 | Warner-Lambert Company | Acides heteroaryle buturiques et leurs derives en tant qu'inhibiteurs de metalloproteinases matricielles |
| AU1110799A (en) | 1997-10-29 | 1999-05-17 | Warner-Lambert Company | Method of inhibiting metastases of cancer cells |
| KR20010033473A (ko) | 1997-12-23 | 2001-04-25 | 로즈 암스트롱, 크리스틴 에이. 트러트웨인 | Ace 저해제-mmp 저해제의 병용 제제 |
| US6169103B1 (en) | 1998-03-03 | 2001-01-02 | Warner-Lambert | Fluorine-substituted biphenyl butyric acids and their derivatives as inhibitors of matrix metalloproteinases |
| CN1148361C (zh) | 1998-05-11 | 2004-05-05 | 武田药品工业株式会社 | 羟基亚氨基链烷酸衍生物 |
| US6288063B1 (en) | 1998-05-27 | 2001-09-11 | Bayer Corporation | Substituted 4-biarylbutyric and 5-biarylpentanoic acid derivatives as matrix metalloprotease inhibitors |
| JP4183350B2 (ja) | 1998-10-28 | 2008-11-19 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | フェニルピロリジノン誘導体 |
| US6541521B1 (en) | 1999-07-12 | 2003-04-01 | Warner-Lambert Company | Benzene butyric acids and their derivatives as inhibitors of matrix metalloproteinases |
| US6518435B1 (en) | 1999-10-29 | 2003-02-11 | Takeda Chemical Industries, Ltd. | Process for the preparation of oxyiminoalkanoic acid derivatives |
| AU1303201A (en) | 1999-11-10 | 2001-06-06 | Takeda Chemical Industries Ltd. | Alkoxyiminoalkanoic acid derivatives |
| HUP0203837A2 (hu) | 1999-11-10 | 2003-03-28 | Takeda Chemical Industries, Ltd. | Testtömegnövekedést gátló szerek |
| GB0003671D0 (en) | 2000-02-17 | 2000-04-05 | Univ Cardiff | Diphenyl-substituted lower alkanes |
| AU2002215218A1 (en) | 2000-11-17 | 2002-05-27 | Takeda Chemical Industries Ltd. | Isoxazole derivatives |
| CZ20031751A3 (cs) | 2000-12-21 | 2004-03-17 | Glaxo Group Limited | Makrolidy |
| US6610723B2 (en) | 2001-01-29 | 2003-08-26 | Hoffmann-La Roche Inc. | Imidazole derivatives |
| JP2002241358A (ja) | 2001-02-15 | 2002-08-28 | Nippon Soda Co Ltd | オキシム基を有する化合物及び殺虫・殺ダニ剤 |
| CA2450589C (fr) | 2001-06-08 | 2011-12-20 | Cytokine Pharmasciences, Inc. | Composes d'isoxazoline presentant une activite d'antagoniste mif |
| US6552188B2 (en) | 2001-06-29 | 2003-04-22 | Kowa Co., Ltd. | Unsymmetrical cyclic diamine compound |
| AR037233A1 (es) | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
| AU2002341921B2 (en) | 2001-10-04 | 2007-05-31 | Merck Sharp & Dohme Corp. | Heteroaryl substituted tetrazole modulators of metabotropic glutamate receptor-5 |
| DE60223720T2 (de) | 2001-12-18 | 2008-10-30 | Merck & Co., Inc. | Heteroaryl-substituierte pyrazol-modulatoren des metabotropen glutamatrezeptors-5 |
| US6949542B2 (en) | 2002-02-06 | 2005-09-27 | Hoffman-La Roche Inc. | Dihydro-benzo[b][1,4]diazepin-2-one derivatives |
| CN1703395A (zh) | 2002-08-09 | 2005-11-30 | 特兰斯泰克制药公司 | 芳基和杂芳基化合物以及调节凝血的方法 |
| AU2003266528A1 (en) | 2002-09-20 | 2004-04-08 | Takeda Pharmaceutical Company Limited | Cyclic amine compound, process for producing the same, and use |
| WO2004032933A1 (fr) | 2002-10-11 | 2004-04-22 | Kowa Co., Ltd. | Methode permettant de traiter le cancer |
| AR042052A1 (es) | 2002-11-15 | 2005-06-08 | Vertex Pharma | Diaminotriazoles utiles como inhibidores de proteinquinasas |
| BRPI0316732B8 (pt) | 2002-11-27 | 2021-05-25 | Incyte Corp | composto derivado de 3-aminopirrolidina e sua composição farmacêutica |
| US7427632B2 (en) | 2002-12-30 | 2008-09-23 | Eli Lilly And Company | Factor Xa inhibitors |
| EP1608622A4 (fr) | 2003-03-24 | 2009-04-01 | Merck & Co Inc | Heterocycles a 6 elements a substitution biaryle en tant que bloqueurs des canaux sodiques |
| CN1566065A (zh) | 2003-06-27 | 2005-01-19 | 中国医学科学院药物研究所 | α位杂原子取代的γ芳基丁本酮酸衍生物及其制法和其药物组合物与用途 |
| SE0301963D0 (sv) | 2003-07-02 | 2003-07-02 | Astrazeneca Ab | New compounds |
| JP2007500128A (ja) | 2003-07-25 | 2007-01-11 | アムジエン・インコーポレーテツド | 置換複素環式化合物及び使用方法 |
| US7420083B2 (en) | 2003-09-25 | 2008-09-02 | Wyeth | Substituted aryloximes |
| US20070099938A1 (en) | 2003-10-24 | 2007-05-03 | Ono Pharmaceutical Co., Ltd. | Antistress drug and medical use thereof |
| CA2540342A1 (fr) | 2003-10-31 | 2005-05-12 | Neurogen Corporation | Agonistes des recepteurs de la capsicine |
| JP2007524682A (ja) | 2004-02-12 | 2007-08-30 | メルク エンド カムパニー インコーポレーテッド | 代謝調節型グルタミン酸受容体−5の調節物質としてのビピリジルアミド |
| GB0403155D0 (en) | 2004-02-12 | 2004-03-17 | Vernalis Res Ltd | Chemical compounds |
| EP1727542A4 (fr) | 2004-03-26 | 2009-08-05 | Cytokine Pharmasciences Inc | Composes, compositions, procedes de fabrication, et procedes d'utilisation destines inhiber le facteur d'inhibition de la migration des macrophages |
| PT1763517E (pt) | 2004-06-28 | 2011-07-01 | Hoffmann La Roche | Derivados de pirimidina como inibidores 11beta-hsd1 |
| JP2008510766A (ja) | 2004-08-27 | 2008-04-10 | ゲーペーツェー ビオテック アーゲー | ピリミジン誘導体 |
| KR20070045272A (ko) | 2004-08-27 | 2007-05-02 | 아스텔라스세이야쿠 가부시키가이샤 | 2-페닐피리딘 유도체 |
| NZ555326A (en) | 2004-12-07 | 2010-01-29 | Toyama Chemical Co Ltd | Novel anthranilic acid derivative or salt thereof |
| US20060178388A1 (en) | 2005-02-04 | 2006-08-10 | Wrobleski Stephen T | Phenyl-substituted pyrimidine compounds useful as kinase inhibitors |
| US7468383B2 (en) | 2005-02-11 | 2008-12-23 | Cephalon, Inc. | Proteasome inhibitors and methods of using the same |
| US7893267B2 (en) | 2005-03-14 | 2011-02-22 | High Point Pharmaceuticals, Llc | Benzazole derivatives, compositions, and methods of use as β-secretase inhibitors |
| EP2605013A1 (fr) | 2005-06-07 | 2013-06-19 | The Rockefeller University | Stimulation de la prolifération des cellules pancréatiques bêta |
| US20070037865A1 (en) | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
| EP1912970A2 (fr) | 2005-08-10 | 2008-04-23 | Bayer Schering Pharma Aktiengesellschaft | Acyltryptophanols pour controle de fertilité |
| US20070060573A1 (en) | 2005-08-10 | 2007-03-15 | Lars Wortmann | Acyltryptophanols |
| CA2619101A1 (fr) | 2005-08-23 | 2007-03-01 | Irm Llc | Composes immunosuppresseurs et compositions associees |
| TW200745055A (en) | 2005-09-23 | 2007-12-16 | Organon Nv | 4-Phenyl-6-substituted-pyrimidine-2-carbonitrile derivatives |
| EP2395002B1 (fr) | 2005-11-08 | 2014-06-18 | Vertex Pharmaceuticals Inc. | Composition pharmaceutique contenant un modulateur hétérocyclique de transporteurs de cassette à liaison atp |
| JP2009518442A (ja) | 2005-12-05 | 2009-05-07 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 可溶性エポキシド加水分解酵素インヒビターとして有益な置換ピラゾール化合物 |
| EP1966141A1 (fr) | 2005-12-14 | 2008-09-10 | Brystol-Myers Squibb Company | Heterocycles a six elements utiles en tant qu inhibiteurs de serine protease |
| WO2007087637A2 (fr) | 2006-01-26 | 2007-08-02 | Washington State University Research Foundation | Compositions et méthodes utilisant des inhibiteurs de métalloprotéinases matrices (mmp) pour traiter des troubles cognitifs caractérisés par une expression et/ou une activité persistante ou soutenue des métalloprotéases |
| US7951824B2 (en) | 2006-02-17 | 2011-05-31 | Hoffman-La Roche Inc. | 4-aryl-pyridine-2-carboxyamide derivatives |
| ES2303758B1 (es) * | 2006-02-20 | 2009-08-13 | Laboratorios Almirall S.A. | Nuevos derivados de piridin-3-amina. |
| JP2007230963A (ja) | 2006-03-03 | 2007-09-13 | Daiso Co Ltd | 2,4−ジ置換ピリジンの製造法 |
| EP2044005B8 (fr) | 2006-06-26 | 2012-12-05 | Warner Chilcott Company, LLC | Inhibiteurs de la prolyl hydroxylase et procédés d'utilisation |
| ES2301380B1 (es) * | 2006-08-09 | 2009-06-08 | Laboratorios Almirall S.A. | Nuevos derivados de 1,7-naftiridina. |
| TW200824689A (en) | 2006-08-10 | 2008-06-16 | Glaxo Group Ltd | Novel compounds |
| US8071631B2 (en) | 2006-08-16 | 2011-12-06 | The J. David Gladstone Institutes, A Testamentary Trust Established Under The Will Of J. David Gladstone | Small molecule inhibitors of kynurenine-3-monooxygenase |
| WO2008022281A1 (fr) | 2006-08-16 | 2008-02-21 | The J. David Gladstone Institutes, A Testamentary Trust Established Under The Will Of J. David Gladstone | Inhibiteurs à petites molécules de kynurénine-3-monooxygénase |
| WO2008023720A1 (fr) | 2006-08-23 | 2008-02-28 | Astellas Pharma Inc. | COMPOSÉ D'URÉE OU SEL DUDIT COMPOSé |
| US8188113B2 (en) | 2006-09-14 | 2012-05-29 | Deciphera Pharmaceuticals, Inc. | Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
| US20080077419A1 (en) | 2006-09-27 | 2008-03-27 | Santiago Pamela M | System And Method For Training Employees Of An Organization To Align Their Job Activities To Achieving The Organization's Strategic Objectives |
| US8735411B2 (en) | 2006-10-02 | 2014-05-27 | Abbvie Inc. | Macrocyclic benzofused pyrimidine derivatives |
| JP5190062B2 (ja) | 2006-10-12 | 2013-04-24 | ノバルティス アーゲー | Iap阻害剤としてのピロリジン誘導体 |
| WO2008095852A1 (fr) | 2007-02-08 | 2008-08-14 | Respiratorius Ab | Arylamides bronchorelaxantes |
| KR20100016073A (ko) | 2007-04-02 | 2010-02-12 | 인스티튜트 포 원월드 헬스 | Cftr 억제제 화합물 및 이의 용도 |
| EP2002834A1 (fr) | 2007-06-13 | 2008-12-17 | Bayer Schering Pharma Aktiengesellschaft | Aryle/hétarylamides en tant que modulateurs du récepteur EP2 |
| TWI444379B (zh) | 2007-06-29 | 2014-07-11 | Sunesis Pharmaceuticals Inc | 有用於作為Raf激酶抑制劑之化合物 |
| PE20091309A1 (es) | 2007-12-21 | 2009-09-30 | Astrazeneca Ab | Derivados de ciclohexilo como inhibidores de acetil coenzima a carboxilasa |
| JP2009280521A (ja) | 2008-05-22 | 2009-12-03 | Daiso Co Ltd | 2,4−ジ置換ピリジンの製造法 |
| JP2011184298A (ja) | 2008-06-02 | 2011-09-22 | Sanwa Kagaku Kenkyusho Co Ltd | 新規化合物及びその医薬用途 |
| EP2321274A1 (fr) | 2008-07-08 | 2011-05-18 | Boehringer Ingelheim International GmbH | Composés pyrrolidinylique et pipéridinylique utiles comme inhibiteurs de nhe-1 |
| US20110230428A1 (en) | 2008-07-22 | 2011-09-22 | John Wityak | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| CA2732806A1 (fr) * | 2008-08-04 | 2010-02-11 | John Wityak | Certains inhibiteurs de kynurenine-3-monooxygenase, compositions pharmaceutiques, et procedes d'utilisation de ceux-ci |
| US8691824B2 (en) | 2008-08-04 | 2014-04-08 | Chdi Foundation, Inc. | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| WO2010075270A1 (fr) * | 2008-12-22 | 2010-07-01 | Incyte Corporation | 2-amino-pyrimidines 4,6-disubstituées, convenant comme modulateurs du récepteur h4 de l'histamine |
| WO2010100475A1 (fr) | 2009-03-02 | 2010-09-10 | Astrazeneca Ab | Dérivés de l'acide hydroxamique en tant qu'agents contre des bactéries à gram négatif |
| US8415378B2 (en) | 2009-04-07 | 2013-04-09 | Astrazeneca Ab | Isoxazol-3(2H)-one analogs as therapeutic agents |
| US20120041009A1 (en) | 2009-05-18 | 2012-02-16 | Sumitomo Chemical Company, Limited | Pyrimidine compound and its use in pest control |
| TWI598347B (zh) | 2009-07-13 | 2017-09-11 | 基利科學股份有限公司 | 調節細胞凋亡信號之激酶的抑制劑 |
| JP5099731B1 (ja) | 2009-10-14 | 2012-12-19 | メルク・シャープ・アンド・ドーム・コーポレーション | p53活性を増大する置換ピペリジン及びその使用 |
| WO2011050323A1 (fr) | 2009-10-22 | 2011-04-28 | The Washington University | Composés et méthodes pour le traitement d'infections bactériennes |
| WO2011060321A1 (fr) | 2009-11-16 | 2011-05-19 | Chdi, Inc. | Inhibiteurs de transglutaminase tg2, compositions pharmaceutiques et leurs procédés d'utilisation |
| PH12012501480A1 (en) | 2010-01-25 | 2012-10-22 | Chdi Foundation Inc | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| CA2791100C (fr) | 2010-02-27 | 2018-01-30 | Bayer Intellectual Property Gmbh | Aryltriazolone liee a un bis-aryle et son utilisation |
| SI2588475T1 (sl) | 2010-07-02 | 2015-12-31 | Gilead Sciences, Inc. | Kinazni inhibitorji za regulacijo apoptoznega signala |
| BR112013006272A2 (pt) | 2010-09-17 | 2019-09-24 | Purdue Pharma Lp | compostos de piridina e seus usos |
| WO2013016488A1 (fr) | 2011-07-28 | 2013-01-31 | Celia Dominguez | Certains inhibiteurs de kynurénine-3-mono-oxygénase, compositions pharmaceutiques et leurs procédés d'utilisation |
| WO2013033068A1 (fr) | 2011-08-30 | 2013-03-07 | Stephen Martin Courtney | Inhibiteurs de kynurénine-3-monooxygénase, compositions pharmaceutiques et procédés d'utilisation de ces compositions |
| SI2750677T1 (sl) | 2011-08-30 | 2017-10-30 | Chdi Foundation, Inc. | Inhibitorji kinurenin-3-monooksigenaze, farmacevtski sestavki in postopki njihove uporabe |
| US9822058B2 (en) | 2012-04-05 | 2017-11-21 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
-
2012
- 2012-08-28 WO PCT/US2012/052617 patent/WO2013033068A1/fr not_active Ceased
- 2012-08-28 PH PH1/2014/500472A patent/PH12014500472A1/en unknown
- 2012-08-28 CA CA2844521A patent/CA2844521A1/fr not_active Abandoned
- 2012-08-28 SG SG2014011654A patent/SG2014011654A/en unknown
- 2012-08-28 CN CN201280042473.7A patent/CN103827095A/zh active Pending
- 2012-08-28 MX MX2014002459A patent/MX2014002459A/es unknown
- 2012-08-28 JP JP2014528512A patent/JP2014525443A/ja not_active Withdrawn
- 2012-08-28 EP EP12827656.5A patent/EP2751086A4/fr not_active Withdrawn
- 2012-08-28 EA EA201490279A patent/EA201490279A1/ru unknown
- 2012-08-28 KR KR1020147005660A patent/KR20140072037A/ko not_active Withdrawn
- 2012-08-28 BR BR112014004845A patent/BR112014004845A2/pt not_active Application Discontinuation
- 2012-08-28 HK HK15100098.4A patent/HK1199726A1/xx unknown
- 2012-08-28 AU AU2012300246A patent/AU2012300246A1/en not_active Abandoned
- 2012-08-28 US US14/241,699 patent/US9428464B2/en active Active
- 2012-08-29 TW TW101131295A patent/TW201326138A/zh unknown
- 2012-08-29 AR ARP120103186A patent/AR087711A1/es unknown
-
2014
- 2014-02-13 ZA ZA2014/01117A patent/ZA201401117B/en unknown
- 2014-03-02 IL IL231271A patent/IL231271A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013033068A1 (fr) | 2013-03-07 |
| ZA201401117B (en) | 2017-09-27 |
| JP2014525443A (ja) | 2014-09-29 |
| CN103827095A (zh) | 2014-05-28 |
| NZ621357A (en) | 2015-07-31 |
| US9428464B2 (en) | 2016-08-30 |
| EP2751086A4 (fr) | 2015-09-16 |
| EP2751086A1 (fr) | 2014-07-09 |
| US20140329795A1 (en) | 2014-11-06 |
| PH12014500472A1 (en) | 2014-05-12 |
| EA201490279A1 (ru) | 2014-08-29 |
| BR112014004845A2 (pt) | 2017-04-04 |
| TW201326138A (zh) | 2013-07-01 |
| MX2014002459A (es) | 2014-04-10 |
| AR087711A1 (es) | 2014-04-09 |
| HK1199726A1 (en) | 2015-07-17 |
| KR20140072037A (ko) | 2014-06-12 |
| AU2012300246A1 (en) | 2014-03-06 |
| IL231271A0 (en) | 2014-04-30 |
| CA2844521A1 (fr) | 2013-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ZA201401117B (en) | Kynurenine-3-monooxygenase inhibitors,pharmaceutical compositions,and methods of use thereof | |
| IL253911A0 (en) | Inhibitors of kynurenine-3-monooxygenase, pharmaceutical compositions, and methods of their use | |
| ZA201206223B (en) | Certain kynurenine-3-monooxygenase inhibitors,pharmaceutical compositions, and methods of use thereof | |
| IL230705A0 (en) | Certain inhibitors of kynurenine-3-monooxygenase pharmaceutical compositions, and methods of their use | |
| IL234884A0 (en) | Inhibitors of kynurenine-3-monooxygenase pharmaceutical compositions, and methods of their use | |
| IL250824B (en) | Certain amino-pyrimidines, their assemblies, and methods of using them | |
| EP2678018A4 (fr) | Combinaison d'inhibiteurs des kinases et utilisations associées | |
| EP2675471A4 (fr) | Compositions liées à la sérumalbumine humaine et procédés d'utilisation | |
| EP2542074A4 (fr) | Agents pharmaceutiques combinatoires au titre d'inhibiteurs de la réplication du vhc | |
| SG10201707020TA (en) | Substituted 3-haloallylamine inhibitors of ssao and uses thereof | |
| IL230917A (en) | 1dyrk inhibitors and their uses | |
| ZA201403431B (en) | Pharmaceutical compositions and methods of use of 4-pregenen-11b-21-triol-3,20-dione derivatives | |
| IL227924A0 (en) | Preparations and methods of use for determining a4he | |
| ZA201402820B (en) | Pharmaceutical compositions comprising dgla and/or 15-hetre and methods of use thereof | |
| EP3049389A4 (fr) | Inhibiteurs de kynurénine-3-monooxygénase, compositions pharmaceutiques et procédés d'utilisation de ceux-ci | |
| ZA201306905B (en) | Novel octahydrothienoquinonline derivative,pharmaceutical composition comprising derivative, and use of these | |
| EP3049077A4 (fr) | Inhibiteurs de kynurénine-3-monooxygénase, compositions pharmaceutiques et procédés d'utilisation de ces compositions | |
| EP2701689A4 (fr) | Compositions pharmaceutiques de raltégravir, procédés de préparation et utilisation de celles-ci | |
| IL228439A0 (en) | Gallium compounds, medical preparations and methods of use | |
| HK1177101A (en) | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof | |
| HK1192727A (en) | Combination of kanase inhibitors and uses thereof |